Peter Dziezok
Procter & Gamble
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Peter Dziezok.
Chemsuschem | 2018
Matthias Kehrer; Julian Mehler; Nicola Taccardi; Jens Nagengast; Julian Kadar; Dimitris Ioannis Collias; Peter Dziezok; Peter Wasserscheid
A convenient and highly efficient way of synthesizing 2-bromopropionic acid (2-BrPA) from lactide is presented. The procedure uses ionic liquids obtained from the addition of HBr to ammonium-based zwitterions as the solvent and bromination agent. The buffered HBr acidity, high polarity, and charge stabilizing character of the ionic liquid (IL) enable the synthesis of 2-BrPA with excellent selectivity. The best results are obtained with an imidazolium-based IL, that is, 1-(4-butanesulfonic acid)-3-methylimidazolium bromide ([MIMBS]Br). The HBr loading and water content of the IL are crucial parameters for the bromination reaction. The formed 2-BrPA product can be selectively isolated by extraction from the IL, and the unconverted substrate remains in the [MIMBS]Br IL for the next run. Successful recycling of the IL over four cycles is demonstrated.
Chemsuschem | 2018
Jens Nagengast; Simon Hahn; Nicola Taccardi; Matthias Kehrer; Julian Kadar; Dimitris Ioannis Collias; Peter Dziezok; Peter Wasserscheid
A new reaction system for the highly selective, hydrobromic acid catalyzed conversion of lactide into acrylic acid under mild conditions is reported. The applied liquid reaction system consists of a temperature-stable bromide-containing ionic liquid and 2-bromopropionic acid as a source of dry HBr, with no volatile organic solvent being used. This allows for the in situ removal of the formed acrylic acid, leading to an unmatched acrylic acid selectivity of over 72 % at full lactide conversion. Accounting for leftover reaction intermediates on the way to acrylic acid, which could be recycled in an elaborate continuous process, the proposed reaction system shows potential for acrylic acid yields well above 85 % in the liquid phase. This opens new avenues for the effective conversion of biogenic lactic acid (e.g., obtained by fermentation from starch) to acrylic acid. The resulting bio-acrylic acid is a highly attractive product for, for example, the diaper industry, where we expect consumers to be especially sensitive to aspects of sustainability.
Archive | 2008
Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig
Archive | 2008
Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig
Archive | 2008
Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig; Martin Werner Frank
Archive | 2008
Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig
Archive | 2009
Harald Hermann Hundorf; Miguel Brandt Sanz; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig
Archive | 2008
Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig
Archive | 2008
Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig
Archive | 2008
Gregory Ashton; Harald Hermann Hundorf; Holger Beruda; Horst Blessing; Peter Dziezok; Axel Krause; Mattias Schmidt; Lutz Stelzig